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SLC36A2

solute carrier family 36 member 2

HCNC Approved Symbol
SLC36A2 (HGNC:18762)
Genomic Coordinates
5:151,314,972 - 151,347,559 (5q33.1)
Synonyms
PAT2, tramdorin, TRAMD1
Disease Associations
This gene is associated with the following 2 diseases in OMIM.

Diagnosed Cases

4Patients

In total, 4 patients were diagnosed with a variant in the SLC36A2 gene.

Frequently observed phenotypes

(Top 5 only, Patient count*)
*% of total patients presenting each phenotype is shown in parentheses.

Hearing loss
 4 (100.0%)
SLC36A2 - Gene browser | 3billion